| NDC Code | 17856-0831-2 |
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| Package Description | 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0831-2) / 30 g in 1 CUP, UNIT-DOSE |
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| Product NDC | 17856-0831 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sodium Polystyrene Sulfonate |
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| Non-Proprietary Name | Sodium Polystyrene Sulfonate |
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| Dosage Form | POWDER, FOR SUSPENSION |
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| Usage | ORAL; RECTAL |
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| Start Marketing Date | 20170207 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090313 |
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| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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| Substance Name | SODIUM POLYSTYRENE SULFONATE |
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| Strength | 4.1 |
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| Strength Unit | meq/g |
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